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Thesis Info

Author

Bilal Khalid; Dilawar Hayat, M.; Atif Javaid

Supervisor

Muhammad Asif Subhani

Department

UMT. Department of Computer Science

Program

BS

Institute

University of Management and Technology

Institute Type

Private

City

Lahore

Province

Punjab

Country

Pakistan

Thesis Completing Year

2015

Thesis Completion Status

Completed

Page

86 . CD

Language

English

Other

Report presented in partial requirement for BS degree Advisor: Muhammad Asif-Subhani; EN; Call No: TP 005.740222 BIL-V

Added

2021-02-17 19:49:13

Modified

2023-02-17 21:08:06

ARI ID

1676713404907

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Synthesis of Nucleobase-Functionalized b-Tripeptide Scaffolds for Higher Ordered Molecular Architectures

The stability of cyclic peptides and their self-assembling ability is an important aspect in the DNA recognition studies. Functionalization of cyclic peptides with nuclear bases may serve the purpose of mimicking and interacting with the DNA single strand. Stacking of the cyclic peptides after functionalzation may develop steric hinderance. L-Lysine, with side chain amino group, was selected to avoid these steric factors. Differently-protected L-lysine was transformed into its respective β-analogue using Arndt Eistert synthesis. These β-amino acids were utilized to synthesize cyclic β-tripeptide scaffolds through a multistep sequence. The scaffolds after deprotection were subjected to functionalization with the selected nuclear bases (adenine, thymine, cytosine and guanine) after conversion to their acetic acid derivatives. The nucleobase-functionalized cyclic β-tripeptide scaffolds were completely deprotected, purified by RP-HPLC and characterized by ESI and HRMS.